Background and aims: Acute intermittent porphyria (AIP) is a rare disorder with diverse clinical presentations, ranging from latent at-risk individuals to recurrent acute attacks with severe complications. Differences between clinical states and risk factors for severe outcomes remain incompletely defined. Approach and results: In this cross-sectional study, personal, biochemical and clinical data were recorded for non-givosiran treated AIP patients across all clinical states by European porphyria expert centres into the European Porphyria Registry during 2012-2018. Logistic regression models assessed associations between clinical factors and outcomes, with disease states defined according to clinical practice at study initiation. Urinary δ-aminolevulinic acid (u-ALA) and porphobilinogen (u-PBG) were normalized to each centre's upper reference limits. Data from 239 participants were included and patients were classified as sporadic attack(s) (n = 61), recurrent (n = 49), in-remission (n = 58), asymptomatic high excreters (n = 23) and latent at-risk (n = 48). Hospitalization for an acute attack was associated with ≥ 10-fold u-PBG increase (adjusted Odds Ratios [aOR] = 22.40, 95% CI = 5.34-94.03), 4-9-fold (6.35 [2.87-14.02]) and ≥ 10-fold (177.50 [8.03-3923]) u-ALA increase, BMI < 18.5 (12.68 [2.86-56.23]) and age 20-39 (4.35 [1.82-10.42]). A 10-fold u-PBG increase (8.22 [2.31-29.28]) and a positive family history at diagnosis (0.30 [0.14-0.64]) were associated with recurrent classification. Recurrent AIP (7.28 [2.77-19.14]) and sporadic heme-treated acute attacks (5.30 [1.89-14.91]) were associated with reduced work capacity and unemployment. Chronic hypertension, chronic kidney disease and primary liver cancer were observed across all clinical groups. Conclusions: In this multicentre European study, we describe disease burden across all clinical AIP states including non-givosiran treated recurrent patients and identify risk factors associated with hospitalization and recurrent disease.
Clinical Characteristics and Outcomes of Acute Intermittent Porphyria: Insights From the European Porphyria Registry / Baravelli, Carl M.; Sandberg, Sverre; Hammersland, Marte H.; Harper, Pauline; Badminton, Michael N.; Aguilera, Paula; Cassiman, David; Deybach, Jean‐charles; Di Pierro, Elena; Graziadei, Giovanna; Langendonk, Janneke G.; Marcacci, Matteo; Sardh, Eliane; Schmitt, Caroline; To‐figueras, Jordi; Ventura, Paolo; Aarsand, Aasne K.. - In: LIVER INTERNATIONAL. - ISSN 1478-3223. - 46:5(2026), pp. 1-17. [10.1111/liv.70615]
Clinical Characteristics and Outcomes of Acute Intermittent Porphyria: Insights From the European Porphyria Registry
Marcacci, MatteoWriting – Review & Editing
;Ventura, PaoloWriting – Review & Editing
;
2026
Abstract
Background and aims: Acute intermittent porphyria (AIP) is a rare disorder with diverse clinical presentations, ranging from latent at-risk individuals to recurrent acute attacks with severe complications. Differences between clinical states and risk factors for severe outcomes remain incompletely defined. Approach and results: In this cross-sectional study, personal, biochemical and clinical data were recorded for non-givosiran treated AIP patients across all clinical states by European porphyria expert centres into the European Porphyria Registry during 2012-2018. Logistic regression models assessed associations between clinical factors and outcomes, with disease states defined according to clinical practice at study initiation. Urinary δ-aminolevulinic acid (u-ALA) and porphobilinogen (u-PBG) were normalized to each centre's upper reference limits. Data from 239 participants were included and patients were classified as sporadic attack(s) (n = 61), recurrent (n = 49), in-remission (n = 58), asymptomatic high excreters (n = 23) and latent at-risk (n = 48). Hospitalization for an acute attack was associated with ≥ 10-fold u-PBG increase (adjusted Odds Ratios [aOR] = 22.40, 95% CI = 5.34-94.03), 4-9-fold (6.35 [2.87-14.02]) and ≥ 10-fold (177.50 [8.03-3923]) u-ALA increase, BMI < 18.5 (12.68 [2.86-56.23]) and age 20-39 (4.35 [1.82-10.42]). A 10-fold u-PBG increase (8.22 [2.31-29.28]) and a positive family history at diagnosis (0.30 [0.14-0.64]) were associated with recurrent classification. Recurrent AIP (7.28 [2.77-19.14]) and sporadic heme-treated acute attacks (5.30 [1.89-14.91]) were associated with reduced work capacity and unemployment. Chronic hypertension, chronic kidney disease and primary liver cancer were observed across all clinical groups. Conclusions: In this multicentre European study, we describe disease burden across all clinical AIP states including non-givosiran treated recurrent patients and identify risk factors associated with hospitalization and recurrent disease.| File | Dimensione | Formato | |
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